7 February 2022

Homozygous exonic and intragenic NRXN1 deletion presenting as either West syndrome or autism spectrum disorder in two siblings

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20 January 2022

Award for our paper “An Overview of Epileptic Encephalopathies Based on Advances in Genetics: A Cohort Study.”

Our paper titled “An Overview of Epileptic Encephalopathies Based on Developments in Genetics: A Cohort Study” got the “Oral Paper Award”  at the “23rd National Child […]
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19 January 2022

COVID-19: pathogenesis, genetic polymorphism, clinical features and laboratory findings

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31 December 2021

Stress-induced childhood onset neurodegeneration with ataxia and seizures (CONDSIAS) presenting with torticollis attacks: Phenotypic variability of the same mutation in two turkish patients

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